His scientific interests lie mostly in Genetics, Mitochondrial DNA, Mutation, Molecular biology and Gene. Min-Xin Guan regularly links together related areas like Hearing loss in his Genetics studies. His Mitochondrial DNA research is multidisciplinary, incorporating elements of Phenotype, Mitochondrial ribosome, Signal transduction and Sequence analysis.
His study explores the link between Molecular biology and topics such as RNA that cross with problems in Aminoglycoside. His Mutation research incorporates elements of Penetrance, Neomycin and Haplogroup. His Penetrance research includes themes of Expressivity and Haplotype.
Min-Xin Guan focuses on Genetics, Mitochondrial DNA, Mutation, Haplogroup and Penetrance. While the research belongs to areas of Genetics, Min-Xin Guan spends his time largely on the problem of Hearing loss, intersecting his research to questions surrounding Nonsyndromic deafness. Min-Xin Guan interconnects Molecular biology, Transfer RNA, Sequence analysis, Mitochondrion and Haplotype in the investigation of issues within Mitochondrial DNA.
His Mutation study frequently links to related topics such as Phenotype. The various areas that Min-Xin Guan examines in his Haplogroup study include Proband, Point mutation, Homoplasmy, Age of onset and Human mitochondrial DNA haplogroup. Penetrance is closely attributed to Expressivity in his research.
Min-Xin Guan spends much of his time researching Argon, Dark matter, Mitochondrial DNA, Mutation and Mitochondrion. The study incorporates disciplines such as Neutrino and DarkSide in addition to Dark matter. His Mitochondrial DNA study is concerned with the field of Genetics as a whole.
Within one scientific family, Min-Xin Guan focuses on topics pertaining to Hearing loss under Genetics, and may sometimes address concerns connected to Point mutation. His Mutation research is multidisciplinary, relying on both Transfer RNA and Mutant. As a member of one scientific family, he mostly works in the field of Mitochondrion, focusing on Retinal ganglion and, on occasion, ATP synthase.
His primary areas of study are Time projection chamber, Mutation, Mitochondrial DNA, Argon and Mitochondrion. In Time projection chamber, Min-Xin Guan works on issues like Dark matter, which are connected to Nuclear physics and Cosmic ray. The concepts of his Mitochondrial DNA study are interwoven with issues in Molecular biology and Mutant.
His Mitochondrion study is focused on Genetics in general. His work on Mitochondrial disease, Gene, Atrophy and DNA repair as part of general Genetics study is frequently connected to Ferredoxin-NADP+ reductase activity, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His Mitochondrial translation research incorporates themes from Penetrance, TRNA modification and Mutation.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Observation of Electron-Antineutrino Disappearance at Daya Bay
F. P. An;J. Z. Bai;A. B. Balantekin;H. R. Band.
Physical Review Letters (2012)
Improved measurement of electron antineutrino disappearance at Daya Bay
F. P. An;Q. An;J. Z. Bai;A. B. Balantekin.
Chinese Physics C (2013)
Improved Measurement of Electron Antineutrino Disappearance at Daya Bay
F. P. An;Q. An;J. Z. Bai.
arXiv: High Energy Physics - Experiment (2012)
Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family
Hui Zhao;Ronghua Li;Qiuju Wang;Qingfeng Yan.
American Journal of Human Genetics (2004)
Spectral Measurement of Electron Antineutrino Oscillation Amplitude and Frequency at Daya Bay
F. P. An;A. B. Balantekin;H. R. Band;W. Beriguete.
Physical Review Letters (2014)
First results from the DarkSide-50 dark matter experiment at Laboratori Nazionali del Gran Sasso
P. Agnes;T. Alexander;A. Alton;K. Arisaka.
Physics Letters B (2015)
Measurement of the Reactor Antineutrino Flux and Spectrum at Daya Bay
F. P. An;A. B. Balantekin;H. R. Band;M. Bishai.
(2016)
Biochemical Evidence for Nuclear Gene Involvement in Phenotype of Non-Syndromic Deafness Associated with Mitochondrial 12S rRNA Mutation
Min-Xin Guan;Nathan Fischel-Ghodsian;Giuseppe Attardi.
Human Molecular Genetics (1996)
Low-Mass Dark Matter Search with the DarkSide-50 Experiment
P. Agnes;I. F. M. Albuquerque;T. Alexander;A. K. Alton.
Physical Review Letters (2018)
New Measurement of Antineutrino Oscillation with the Full Detector Configuration at Daya Bay
F. P. An;A. B. Balantekin;H. R. Band;M. Bishai.
Physical Review Letters (2015)
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